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• A highly selective ratiometric fluorescent sensor N-CQDs/AuNCs for carbendaizm was developed. • The sensor has good selectivity and sensitivity to carbendazim with wide dynamic response range. • Sensor avoids the influences caused by probe concentration and drifts of optoelectronic system. • The ratiometric fluorescent sensor is a promising candidate for carbendazim detection. A novel fluorescence "turn on" ratiometric fluorescent sensor was employed to determine carbendazim. The sensing process was achieved through the strong fluorescence resonance energy transfer (FRET) between nitrogen doped carbon quantum dots (N-CQDs) and gold nanocluster (AuNCs). The photoluminescence intensity of N-CQDs can be deactivated by AuNCs through FRET effect and recovered by the addition of carbendazim. The ratiometric detection of carbendazim is achieved by recording the photoluminescence and second-order Rayleigh scattering (SRS) signal of N-CQDs/AuNCs system. With the introduction of carbendazim to the sensing platform resulted in the photoluminescence and SRS signal of N-CQDS/AuNCs enhancing. UV–vis absorption, Zeta potential and fluorescence lifetime analyses indicate that the fluorescence turn on process can be attributed to the aggregation of AuNCs breaks the FRET process and increases SRS intensity. N-CQDs/AuNCs probe present a good sensitivity and selectivity for carbendazim detection, with two linear response ranges (1−100 μM, 150−1000 μM), low detection limit of 0.83 μM and 37.25 μM. Furthermore, real sample analyses indicate that the as-presented sensor has potentials in carbendazim determination in real sample analyses. [ABSTRACT FROM AUTHOR]

A new high performance fluorescence assay for detection of Ag+ based on CdS quantum dots (QDs) using L-Aspartic acid (L-Asp) as a stabilizer was proposed in this work. The CdS quantum dots conjugation with L-Aspartic acid (L-Asp@CdS QDs) were successfully synthesized via a simple hydrothermal process. The QDs have a fluorescence emission band maximum at 595 nm with a quantum yield of 11%. The obtained CdS QDs exhibit a particle size of 1.63 ± 0.28 nm and look like quantum dot flowers. Basically, the fluorescence intensity of L-Asp@CdS QDs can be enhanced only upon addition of Ag+ and a redshift in the fluorescence spectrum was observed. Under optimum conditions, the fluorescence enhancement of L-Asp@CdS QDs appeared to exhibit a good linear relationship in between 100–7000 nM (R2 = 0.9945) with the Ag+ concentration, with a detection limit of 39 nM. The results indicated that the L-Asp@CdS QDs were well used in detection for Ag+ as fluorescence probe in aqueous solution with high sensitivity and selectivity. Moreover, the sensing system has been applied in detection Ag+ in real water samples. The recovery test results were 98.6%~113%, and relative standard deviation (n = 5) is less than 3.6%, which was satisfactory. [ABSTRACT FROM AUTHOR]

Citric acid capped CdS quantum dots (CA-CdS QDs), a new assembled fluorescent probe for copper ions (Cu2+), was synthesized successfully by a simple hydrothermal method. In this work, the fluorescence sensor for the detection of heavy and transition metal (HTM) ions has been extensively studied in aqueous solution. The results of the present study indicate that the obtained CA-CdS QDs could detect Cu2+ with high sensitivity and selectivity. It found that the existence of Cu2+ has a significant fluorescence quenching with a large red shifted (from greenish-yellow to yellowish-orange), but not in the presence of 17 other HTM ions. As a result, Cu2S, the energy level below the CdS conduction band, could be formed at the surface of the CA-CdS QDs and leads to the quenching of fluorescence of CA-CdS QDs. Under optimal conditions, the copper ions detection range using the synthesized fluorescence sensor was 1.0 × 10‒8 M to 5.0 × 10‒5 M and the limit of detection (LOD) is 9.2 × 10‒9 M. Besides, the as-synthesized CA-CdS QDs sensor exhibited good selectivity toward Cu2+ relative to other common metal ions. Thus, the CA-CdS QDs has potential applications for detecting Cu2+ in real water samples. [ABSTRACT FROM AUTHOR]

Abstract Water-soluble rhodamine B assisted graphene quantum dots (RhB-GQDs) were synthesized by a facile one-pot hydrothermal method, using rhodamine B and ethylenediamine as nitrogen source. The as-synthesized RhB-GQDs have few layers configuration with an average size of 4.5 nm and good distribution. The fluorescence quenching approach was applied to the sensing of mercury ions in water. Rodamine B absorb on the surface of RhB-GQDs, and it can prevent RhB-GQDs from contacting with interfering cations. The presence of N atoms reduces the ability of interfering cations to form stable complex with carboxyl groups, and gives the RhB-GQDs good selectivity to mercury ions. In the case of low concentration, the fluorescence quenching efficiency of as-synthesized RhB-GQDs still has a good liner relationship with concentration. Due to the strong affinity of Hg2+ to amino and carboxyl on the surface of RhB-GQDs, the fluorescence of RhB-GQDs is quenched by nonradiative electron transfer between Hg2+ and the excited state of RhB-GQDs. Based on the fluorescence turn off process, the as-synthesized RhB-GQDs can be served as fluorescent platform for the sensitive and selective detection of Hg2+ with a detection limit of 0.16 nM. Graphical abstract Rhodamine B assisted graphene quantum dots (RhB-GQDs) synthesized a facile one-pot hydrothermal method using rhodamine B and ethylenediamine as nitrogen source exhibit the excellently selective and sensitive response to Hg2+ as flourescent sensor. fx1 [ABSTRACT FROM AUTHOR]

This work uses ZnO nanoparticles as the probe and a case, proving that the grey level can replace fluorescent intensity to realize a quantitative detection function of paper-based Cu 2+ sensor. Portable Cu 2+ test papers were obtained through dipping filter papers in as-prepared ZnO sol possessing the Cu 2+ quenching property. Based on grey level which is obtained through ordinary digital camera and computer, the detection function of the fabricated Cu 2+ test paper is extended from qualitative detection relied on naked eyes to quantitative detection whose detection range is calculated to be 10–1000 μM. The fabricated test papers also could resist the interruption of some competing ions and is a potential candidate for portable Cu 2+ detection device with quantitative function. Since the strategy of replacing fluorescence intensity by grey level is based on the map relationship between the fluorescence intensity and the digital signal (grey level), it is promising to be applied to other fluorescent test papers to gain quantitative test papers aimed at corresponding chemicals. At the same time, the mechanism of Cu 2+ -induced fluorescence quenching was also investigated by fluorescence lifetime, UV–vis spectra, and photoluminescence spectra. And a static quenching mechanism based on the non-fluorescence complex formed by Cu 2+ and O x − is brought up. [ABSTRACT FROM AUTHOR]